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rs876660678

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660678(A;A)
Make rs876660678(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23626354
GenePALB2
is asnp
is mentioned by
dbSNPrs876660678
ebirs876660678
HLIrs876660678
Exacrs876660678
Varsomers876660678
Maprs876660678
PheGenIrs876660678
hapmaprs876660678
1000 genomesrs876660678
hgdprs876660678
ensemblrs876660678
gopubmedrs876660678
geneviewrs876660678
scholarrs876660678
googlers876660678
pharmgkbrs876660678
gwascentralrs876660678
openSNPrs876660678
23andMers876660678
23andMe allrs876660678
SNP Nexus

SNPshotrs876660678
SNPdbers876660678
MSV3drs876660678
GWAS Ctlgrs876660678
Max Magnitude0
ClinVar
Risk rs876660678(A;A)
Alt rs876660678(A;A)
Reference rs876660678(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene PALB2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000016.9:g.23637675C>T
CLNSRC
CLNACC RCV000213186.1,